ChiCTR1800019782.
| Trial name or title | The effect of Intense pulsed light on moderate meibomian gland dysfunction |
| Methods |
Study design: randomised controlled trial Study grouping: parallel group Exclusions after randomisation? Not applicable Percentage of participant follow‐up: not applicable Study duration (of intervention): not reported Was a sample size calculation reported: no |
| Participants |
Baseline characteristics IPL + MGX group
MGX (standard therapy) group
Overall
Inclusion criteria: aged ≥ 18 years; SPEED score ≥ 6 points; eyelid margin obtuse or hypertrophy or new blood vessels; meibomian gland orifices obstruction, uplift or lipid suppository form; meibum quality score of a single eyelid 5–10 points; Schimer test > 5 mm Exclusion criteria: eye infection, surgery or trauma in past 6 months; eyelid closure insufficiency, entropion or ectropion, etc.; Fitzpatrick skin category 5–6; treatment before 4 weeks with a tan or tanning, tender skin treatment or have been too sensitive or allergic symptoms; pretreatment area is skin cancer or pigmentary lesions; in past month have dry eye physical therapy or point with anti‐inflammatory drugs; systemic immune‐related diseases, such as Sjogren's syndrome, Stevens‐Johnson syndrome, rheumatism, etc.; nerve lesions, such as trigeminal nerve tumours, surgery or trauma, virus damage, etc.; people with metabolic diseases such as diabetes mellitus, hypothyroidism and thyroid hyperfunction, etc. Significant pretreatment baseline differences? Not applicable Severity of dry eye: not reported |
| Interventions |
IPL + MGX
Standard therapy only
|
| Outcomes |
Primary outcomes:
|
| Starting date | Recruiting status: recruiting (as of 18 September 2019) |
| Contact information | Study leader: Zeng Qingyan Hankou Aier Eye Hospital, 328 Machang Road, Jianghan District, Wuhan, Hubei, China Email: zengqingyan1972@163.com Telephone: +86 13971009610 |
| Notes | None |